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Fulvestrant in Combination with CDK4/6 Inhibitors for HER2- Metastatic Breast Cancers: Current Perspectives

机译:齐鲁芬特与CDK4 / 6抑制剂联合治疗HER2转移性乳腺癌:当前观点

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摘要

The development of CDK 4/6 inhibitors has dramatically changed the therapeutic management of hormone receptor-positive (HR+) and HER2 negative metastatic breast cancer (MBC). In combination with fulvestrant, palbociclib, ribociclib and abemaciclib have each been approved for HR+/HER2- MBC following the results of randomized Phase III studies (PALOMA-3, MONALEESA-3, MONARCH-2) and shown a significant advantage in PFS. Data from clinical trials support the combination with aromatase inhibitors in the first line setting and with fulvestrant in the second line. Each agent is well tolerated, and most of the toxicities observed with this class of drugs are generally easily manageable and free from particular complications. The latest evidence from MONARCH-2 and MONALEESA-3 trials shows benefits in terms of overall survival (OS), suggesting an option of using fulvestrant in combination with CDK 4/6 inhibitors in the first line setting. Additional research is needed to determine optimal treatment sequencing, understand the mechanisms of resistance, and develop novel therapeutic strategies to overcome clinical resistance and further improve the outcomes of patients with HR+/HER- MBC. Key questions in the field include the further impact on progression-free survival, overall survival, and the role of continuing CDK 4/6 blockade beyond progression. The purpose of this review is to describe the clinical relevance of fulvestrant in combination with CDK 4/6 inhibitors in HR+/HER2- MBC patients, as well as to discuss the current controversies and evolving research areas.
机译:CDK 4/6抑制剂的开发极大地改变了激素受体阳性(HR +)和HER2阴性转移性乳腺癌(MBC)的治疗管理。遵循随机III期研究(PALOMA-3,MONALEESA-3,MONARCH-2)的结果,palbociclib,ribociclib和abemaciclib与氟维司群合用均被批准用于HR + / HER2-MBC,在PFS中显示出显着优势。来自临床试验的数据支持在第一行中将芳香酶抑制剂与第二行中的氟维司群合用。每种药物均具有良好的耐受性,使用此类药物观察到的大多数毒性通常易于控制并且没有特殊并发症。 MONARCH-2和MONALEESA-3试验的最新证据显示,在总体存活率(OS)方面有好处,这表明在一线治疗中可以选择将氟维司群与CDK 4/6抑制剂联合使用。需要其他研究来确定最佳治疗顺序,了解耐药机制,并开发新的治疗策略来克服临床耐药性并进一步改善HR + / HER-MBC患者的结局。该领域的关键问题包括对无进展生存期,总体生存率的进一步影响,以及持续的CDK 4/6阻滞超越进展的作用。这篇综述的目的是描述氟维司群与CDK 4/6抑制剂联合治疗HR + / HER2-MBC患者的临床意义,并讨论当前的争议和不断发展的研究领域。

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